CN117770267A - Mite-killing composition and application thereof - Google Patents

Mite-killing composition and application thereof Download PDF

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Publication number
CN117770267A
CN117770267A CN202311764473.4A CN202311764473A CN117770267A CN 117770267 A CN117770267 A CN 117770267A CN 202311764473 A CN202311764473 A CN 202311764473A CN 117770267 A CN117770267 A CN 117770267A
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active ingredient
acaricidal composition
mites
mass ratio
pyriminostrobin
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Inventor
葛家成
葛晓甜
刘桂娟
刘静
刘金玲
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QINGDAO KAIYUANXIANG CHEMICAL CO Ltd
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QINGDAO KAIYUANXIANG CHEMICAL CO Ltd
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Abstract

The invention belongs to the technical field of pesticide mite killing, and discloses a mite killing composition and application thereof, wherein an active ingredient in the mite killing composition comprises an active ingredient A and an active ingredient B, the active ingredient A is sulfofiflumin, and the active ingredient B is fluazinam or pyriminostrobin. The acaricidal composition has remarkable synergistic effect on controlling phytophagous harmful mites such as panonychus citri and the like, effectively reduces the dosage of pesticides, and is safe to the environment.

Description

Mite-killing composition and application thereof
Technical Field
The invention belongs to the technical field of pesticide mite killing, and discloses a mite killing composition and application thereof.
Background
Fluazinam, CAS accession number 79622-59-6, chemical name 3-chloro-N- [ 3-chloro-2, 6-dinitro-4- (trifluoromethyl) phenyl ] -5- (trifluoromethyl) pyridin-2-amine. The oxidative phosphorylation decoupling agent has excellent control effects on plant diseases such as early blight, late blight and the like, and has certain control effects on mites.
Pyricularia, CAS registry number 1257598-43-8, chemical name (E) -2- [2- [ [2- (2, 4-dichlorophenylamino) -6- (trifluoromethyl) pyrimidin-4-yl ] oxymethyl ] phenyl ] -3-methoxyprop-2-enoic acid methyl ester, belongs to mitochondrial respiratory chain inhibitors.
The phytophagous pest mites are closely related to agricultural production, have the characteristics of multiple species, wide distribution, multiple feeding habits and the like, are recognized pest populations which are difficult to control, and are mainly of the tetranychidae. The phytophagous mites absorb juice on the front or back of the leaves of the plants, so that the transpiration of the water on the leaves is enhanced, the chlorophyll is reduced, the photosynthesis is inhibited, and the leaves are discolored and dry up, and the whole plant is dead when serious.
Agricultural production has long been mainly dependent on chemical control to control large-area outbreak mites, and the problem of drug resistance is more and more prominent due to special ecological countermeasures and environmental adaptability of mites. The use of a large amount of pesticides also aggravates environmental pollution and damages natural ecological balance. Therefore, the applicant compounds the sulfofiflumin with any one of fluazinam or pyriminostrobin, and discovers that the sulfofiflubin has obvious synergistic effect on controlling phytophagous harmful mites, slows down the development of drug resistance of the harmful mites and is safe to the environment.
Disclosure of Invention
Based on the above, the invention aims to provide the acaricidal composition, which has remarkable synergistic effect on controlling the phytophagous harmful mites such as the panonychus citri, effectively reduces the dosage of pesticides and is safe to the environment.
It is another object of the present invention to provide a crop safe acaricidal composition;
in order to achieve the above purpose, the invention adopts the following technical scheme that the active ingredient of the acaricidal composition comprises an active ingredient A and an active ingredient B, wherein the active ingredient A is sulfofiflumin, the active ingredient B is fluazinam or pyriminostrobin, and the mass ratio of the active ingredient to the active ingredient B is 1:30-42:1.
Further, the active ingredient B in the acaricidal composition is fluazinam, and the mass ratio of the active ingredient A to the active ingredient B is 1:30-42:1, such as 1:30, 1:24, 1:12, 1:6, 1:3, 6:1, 10:1, 24:1, 35:1, 42:1 or any value between the above values;
further, the active ingredient B in the acaricidal composition is fluazinam, and the mass ratio of the active ingredient A to the active ingredient B is 1:24-35:1, such as 1:24, 1:12, 1:6, 1:3, 6:1, 10:1, 24:1, 35:1 or any value between the above values;
further, the active ingredient B in the acaricidal composition is pyriminostrobin, and the mass ratio of the active ingredient A to the active ingredient B is 1:28-25:1, such as 1:28, 1:15, 2:9, 2:3, 3:2, 6:1, 12:1, 25:1 or any value between the above values;
further, the active ingredient B in the acaricidal composition is pyriminostrobin, and the mass ratio of the active ingredient A to the active ingredient B is 1:15-12:1, such as 1:15, 2:9, 2:3, 3:2, 6:1, 12:1 or any value between the above values;
further, the acaricidal composition comprises auxiliary components acceptable in pesticides besides active components, wherein the auxiliary components are wetting agents, dispersing agents, emulsifying agents, thickening agents, disintegrating agents, antifreezing agents, antifoaming agents, preservatives, stabilizing agents, synergists, filling agents, solvents or carriers;
further, the wetting agent is one or more of alkylbenzene sulfonate, alkyl naphthalene sulfonate, lignin sulfonate, sodium dodecyl sulfate, dioctyl sodium succinate sulfonate, alpha-olefin sulfonate, alkylphenol ethoxylate, castor oil polyoxyethylene ether, alkylphenol ethoxylate, fatty alcohol polyoxyethylene ether sodium sulfate, silkworm excrement, chinese honeylocust fruit powder, soapberry powder, SOPA, detergent, emulsifier 2000 series and wetting penetrating agent F; and/or
Further, the dispersing agent is one or more of lignosulfonate, alkyl naphthalene sulfonate formaldehyde condensate, naphthalene sulfonate, tristyrylphenol ethoxylate phosphate, fatty alcohol ethoxylate, alkylphenol polyoxyethylene ether methyl ether condensate sulfate, fatty amine polyoxyethylene ether, glycerin fatty acid ester polyoxyethylene ether, polycarboxylate, polyacrylic acid, phosphate, EO-PO block copolymer and EO-PO graft copolymer; and/or
Further, the emulsifier is one or more of calcium dodecyl benzene sulfonate, alkylphenol formaldehyde resin polyoxyethylene ether, phenethyl phenol polyoxyethylene polyoxypropylene ether, fatty alcohol ethylene oxide-propylene oxide copolymer, styrylphenol polyoxyethylene ether, castor oil polyoxyethylene ether and alkylphenol ether phosphate; and/or
Further, the thickener is one or more of xanthan gum, organic bentonite, gum arabic, sodium alginate, magnesium aluminum silicate, carboxymethyl cellulose and white carbon black; and/or
Further, the disintegrating agent is one or more of sodium sulfate, ammonium sulfate, aluminum chloride, sodium chloride, ammonium chloride, bentonite, glucose, sucrose, starch, cellulose, urea, sodium carbonate, sodium bicarbonate, citric acid and tartaric acid; and/or
Further, the antifreezing agent is one or more of alcohols, alcohol ethers, chlorinated hydrocarbons and inorganic salts; and/or
Further, the defoamer is C 10 -C 20 Saturated fatty acid compound, silicone oil, silicone compound, C 8 -C 10 One or more of the fatty alcohols; and/or
Further, the preservative is one or more of propionic acid, sodium propionate, sorbic acid, sodium sorbate, potassium sorbate, benzoic acid, sodium benzoate, sodium p-hydroxybenzoate, methyl p-hydroxybenzoate, pinocembrane and 1, 2-benzisothiazolin-3-one; and/or
Further, the stabilizer is one or more of disodium hydrogen phosphate, oxalic acid, succinic acid, adipic acid, borax, 2, 6-di-tert-butyl-p-cresol, triethanolamine oleate, epoxidized vegetable oil, kaolin, bentonite, attapulgite, white carbon black, talcum powder, montmorillonite and starch; and/or
Further, the synergistic agent is selected from synergistic phosphorus and synergistic ether; and/or
Further, the filler is a solvent, a filler or a carrier;
further, the solvent is one or more of benzene, toluene, xylene, durene, methanol, ethanol, isopropanol, n-butanol, dimethyl sulfoxide, dimethylformamide, cyclohexanone, alkylene carbonate, diesel oil, solvent oil, vegetable oil derivatives and water; and/or
Further, the carrier is one or more of ammonium salt, ground natural mineral, ground artificial mineral, silicate, resin, wax, solid fertilizer, water, organic solvent, mineral oil, vegetable oil and vegetable oil derivative.
Further, the preparation formulation of the acaricidal composition is a solution, a suspending agent, emulsifiable concentrate, aqueous emulsion, microcapsule suspending agent, microemulsion, suspoemulsion, dispersible oil suspending agent, granule, water dispersible granule and wettable powder;
furthermore, the preparation formulation is suspending agent, emulsifiable concentrate, water dispersible granule and wettable powder.
The invention also discloses application of the acaricidal composition to prevention and treatment of phytophagous harmful mites.
Further, the phytophagous harmful mites are tetranychidae harmful mites.
Further, the tetranychus urticae is panonychus citri, panonychus ulmi, tetranychus cinnabarinus or tetranychus urticae.
Further, the acaricidal composition is applied to mites and plants in which they grow or the environment in which they grow.
The beneficial effects of the invention are as follows:
1) The acaricidal composition has obvious synergism for preventing and controlling phytophagous harmful mites at a certain ratio, and particularly has better prevention and control effect on panonychus citri;
2) The acaricidal composition can obviously reduce the population of mites, reduce the harm of mites to crops, improve the quick action of the medicament and delay the development of drug resistance;
3) The acaricidal composition is safe and efficient, and is safe to crops, non-target organisms, beneficial organisms and natural enemies.
Detailed Description
The technical solutions in the examples of the present invention will be clearly and completely described below in connection with the preparation examples and specific examples of the present invention. All other embodiments, which can be made by those skilled in the art based on the embodiments of the invention without making any inventive effort, are intended to be within the scope of the invention.
Preparation example 1:28% sulfaflumin-fluazinam water dispersible granule (1:6)
The formula comprises the following components: 4% of sulfofiflumin, 24% of fluazinam, 10% of naphthalene sulfonic acid formaldehyde polymer sodium salt, 2% of polycarboxylic acid sodium salt, 4% of nekal BX and kaolin are used for the balance;
the preparation method comprises the following steps: adding active ingredients into a carrier according to the formula proportion, adding a surfactant and other functional additives into the carrier, mixing, adding 10-25% of water after jet milling, and then kneading, granulating, drying and screening to obtain a water dispersible granule product; or spraying water, granulating, drying, and sieving to obtain the final product.
Preparation example 2:18% sulfaflumin-fluazinam suspension (8:1)
The formula comprises the following components: 16% of sulfofiflumin, 2% of fluazinam, 2% of alkylphenol ethoxylates, 1% of polycarboxylic acid sodium salt, 4% of alkylphenol ethoxylate phosphate, 2% of alkylaryl polyoxyethylene ether polyoxypropylene ether, 0.5% of magnesium aluminum silicate, 0.25% of xanthan gum, 4% of ethylene glycol, 0.1% of potassium benzoate, 0.5% of silicone oil and deionized water, and the balance being water;
the preparation method comprises the following steps: according to the formula proportion, the active ingredients, the surfactant and other functional auxiliary agents are sequentially placed in a reaction kettle, water is added and mixed uniformly, high-speed shearing and wet sanding are carried out, and finally, the suspending agent product is obtained through homogenizing and filtering.
Preparation example 3:22% sulfofiflumin pyriminostrobin suspension (2:9)
The formula comprises the following components: 4% of sulfofiflumin, 18% of pyriminostrobin, 2% of glycerol fatty acid ester polyoxyethylene ether, 2% of alkylaryl polyoxyethylene ether polyoxypropylene ether, 1% of naphthalene sulfonate formaldehyde condensate, 5% of polyoxyethylene sorbitan monooleate, 1% of magnesium aluminum silicate, 0.1% of carboxyethyl cellulose, 1% of sodium sorbate, 5% of ethylene glycol, 0.4% of silicone oil and deionized water which are used for the balance;
the preparation method comprises the following steps: according to the formula proportion, the active ingredients, the surfactant and other functional auxiliary agents are sequentially placed in a reaction kettle, water is added and mixed uniformly, high-speed shearing and wet sanding are carried out, and finally, the suspending agent product is obtained through homogenizing and filtering.
Preparation example 4:21% sulfofiflumin pyriminostrobin water dispersible granule (6:1)
The formula comprises the following components: 18% of sulfofiflumin, 3% of pyriminostrobin, 8% of dispersing agent MF-5, 2% of sodium polycarboxylate, 2% of sodium dodecyl sulfate and light calcium carbonate are used for the balance.
The preparation method comprises the following steps: adding active ingredients into a carrier according to the formula proportion, adding a surfactant and other functional additives into the carrier, mixing, adding 10-25% of water after jet milling, and then kneading, granulating, drying and screening to obtain a water dispersible granule product; or spraying water, granulating, drying, and sieving to obtain the final product.
Preparation example 5:15% sulfofiflumin pyriminostrobin wettable powder (2:3)
The formula comprises the following components: 6% of sulfofiflumin, 9% of pyriminostrobin, 10% of calcium lignosulfonate, 2% of dispersant NNO, 2% of sodium dodecyl sulfate and kaolin, and the balance being made up;
the preparation method comprises the following steps: the active ingredients, the dispersing agent, the wetting agent and the filler are mixed according to the formula proportion, uniformly stirred in a stirring kettle, and crushed and uniformly mixed for a plurality of times by a jet mill, thus obtaining the wettable powder of the composition.
Example 1: indoor biological virulence Activity assay
The test is based on: test reference NY/T1154.13-2008 "pesticide in laboratory bioassay test guidelines section 13: leaf disk spray method.
Biological test material: citrus red spider (panoneichus citri).
Test agent: a sulfaflumin crude drug, a fluazinam crude drug, and a pyriminostrobin crude drug.
Test preparation: selecting citrus leaves which grow consistently and are not used with any medicament, making leaf discs by using a puncher, placing a wet sponge block in a culture dish, placing filter paper on the wet sponge block, placing leaf discs on the filter paper, inoculating test mites on the leaf discs by using 2 leaf discs in each dish, and inoculating 15 heads of each leaf disc.
And (3) preparation of a medicament: preparing the original organic solvent into mother solution, and preparing 5 series of mass concentrations by using 0.1% Tween 80 aqueous solution according to an equal ratio method.
And (3) medicament treatment: and (3) placing the culture dish on a bottom plate of a potter spray tower for spraying, wherein the spraying amount is 1mL, taking out the culture dish after the medicament is settled for 1min, and transferring the culture dish to a normal condition for feeding. Each treatment was repeated 4 times and treatments without agent (with all organic solvents and emulsifiers) were set as blank.
Feeding and observing: the treated mites were kept and observed at a temperature of (25.+ -. 1) ℃ and a photoperiod of L: D= (16:8) h.
Checking: the death of the test insects was checked 48h after the treatment, and the total mites and the dead mites were recorded, respectively.
The calculation method comprises the following steps:
mortality of each treatment was calculated from the survey data. Calculated according to the following formula:
wherein:
p-mortality in percent (%);
k-represents the number of dead insects in units of heads;
n-represents the total number of insects treated in units of heads.
Wherein:
P 1 -correct mortality in percent (%);
P t mortality rate in percent (%));
P 0 Blank mortality in percent (%).
If the control mortality is less than 5%, correction is not needed; the control mortality is between 5% and 20%, and correction is carried out according to the formula (2); control mortality was > 20% and the test was reworked.
The co-toxicity coefficient (CTC value) of the mixture is calculated according to the formulas (3), (4) and (5):
wherein:
ati—actual measured virulence index of the mixture;
S-LC of Standard acaricide 50 Milligrams per liter (mg/L);
M-LC of the mixture 50 Units are milligrams per liter (mg/L).
TTI=TI A ×P A +TI B ×P B
Wherein:
TTI-the theoretical toxicity index of the mixture;
TI A -a medicament virulence index;
P A -the percentage of agent a in the mix, in percent (%);
TI B -B agent virulence index;
P B the percentage of the B medicament in the mixture is expressed as percentage (%).
Wherein:
ctc—co-toxicity coefficient;
ati—actual measured virulence index of the mixture;
TTI-the theoretical toxicity index of the mixture.
The compound co-toxicity coefficient CTC is more than or equal to 120 and shows synergistic effect; ctc.ltoreq.80 shows antagonism; 80 < CTC < 120 shows additive effect. The results of the indoor toxicity test are shown in the following table:
TABLE 1 results of indoor biological Activity assay of Sulfiflumin and fluazinam on Panonychus citri
Test agent Toxicity regression equation Correlation coefficient R LC 50 (mg/L) Co-toxicity coefficient
Sulfiflumin(A) y=4.3996+1.1979x 0.9864 3.1714 /
Fluazinam (B) y=3.3178+1.2794x 0.9952 20.6438 /
A:B=1:30 y=3.5771+1.2794x 0.9919 12.9476 135.381
A:B=1:24 y=3.6477+1.3110x 0.9966 10.7529 157.315
A:B=1:12 y=3.6724+1.4325x 0.9968 8.4477 171.634
A:B=1:6 y=4.0083+1.2429x 0.9941 6.2789 183.979
A:B=1:3 y=4.1927+1.2235x 0.9954 4.5691 190.050
A:B=6:1 y=4.6808+1.3639x 0.9943 1.7141 210.466
A:B=10:1 y=4.6223+1.3663x 0.9897 1.8899 181.796
A:B=24:1 y=4.6108+1.2646x 0.9980 2.0312 161.605
A:B=35:1 y=4.6044+1.1026x 0.9941 2.2847 142.152
A:B=42:1 y=4.5167+1.1738x 0.9811 2.5807 125.357
A:B=55:1 y=4.4469+1.1477x 0.9915 3.0336 106.147
TABLE 2 results of indoor biological Activity assay of Sulfiflumin and pyriminostrobin on Panonychus citri
As shown in the indoor test results of tables 1-2, the mite-killing composition provided by the invention has a good control effect on panonychus citri. When Sulfiflumin and fluazinam are compounded, the Sulfiflumin and fluazinam show synergistic effect on panonychus ulmi in the mass ratio of 1:30-42:1; the mass ratio is 1:24-35:1, the co-toxicity coefficient is more than 140, and the synergy is obvious; the mass ratio is 1:12-10:1, the co-toxicity coefficient is more than 170, and the synergy is remarkable; and at a mass ratio of 55:1, an additive effect is exhibited.
The Sulfiflumin and the pyriminostrobin are compounded, the mass ratio of the Sulfiflumin to the pyriminostrobin is 1:28-25:1, and the Sulflumin and the pyriminostrobin are shown as synergistic effect; the co-toxicity coefficient is more than 130 when the mass ratio is 1:15-12:1, and the synergy is obvious; the co-toxicity coefficient is greater than 140 when the mass ratio is 1:15-6:1, and the synergy is remarkable; and the mass ratio is 1:42, 30:1-40:1, and the addition effect is shown.
Example 2: pesticide effect control test for controlling citrus red spiders in field
Experimentally: the citrus orchard in yellow rock area of Taizhou, zhejiang province, the test land is a citrus unshiu, the damage of the citrus red spider is serious all year round, all the test areas are uniform and consistent, and the agricultural practice of local science is met.
Test cell setting: the test was set up with a total of 5 agent treatments, 1 clear water control treatment. Each cell was arranged in random groups, the area of each cell treated was 2 citrus trees, and each treatment was repeated 4 times.
Time and method of administration: when the pesticide is applied, a conventional crown spraying method is adopted, a backpack type manual sprayer is used for applying the pesticide to the citrus trees, the pesticide is applied in 2023 and 5 months and 15 days in the test, the weather is normal during the test, and severe weather factors affecting the test result do not appear. The tested medicament is diluted by adding water according to the designed dosage when the medicament is applied, and the medicament is uniformly sprayed until the water drops from leaves when the medicament is applied.
Investigation time and investigation method: the number of the insects was examined before the drug, and the number of the remaining mites was examined 1 time each of 3d, 15d and 30d after the drug, and the total was examined 4 times. Each cell marks 1 tree tip in east, south, west, north and middle of each tree, the top 5 leaves of each tree tip are investigated, the number of active mites on 50 leaves is investigated in total in each cell, and the number of active mites is counted.
The drug effect calculation method comprises the following steps:
and (5) field efficacy test results and analysis:
the investigation result of 3d after the medicine shows that the control effect of the compound acaricide composition to citrus red mites is 87.87 percent and 87.50 percent which are higher than that of each control single dose; after the medicine is taken, the control effects of four medicines, namely, 18 percent of sulfofiflumin-fluazinam suspending agent (8:1) and 15 percent of sulfofiflumin-pyriminostrobin wettable powder (2:3), are 93.46 percent and 92.60 percent respectively; 30d after the medicine, the mite-killing composition has obviously higher control effect on citrus red mites than that of each single dose of control, and has longer lasting period. In the tested concentration range, the acaricidal composition disclosed by the invention has no obvious phytotoxicity phenomenon on citrus leaves, tender tips and fruits after being used.
While the invention has been described in detail in terms of the general description and the specific embodiments, it will be apparent to those skilled in the art that various modifications and improvements can be made thereto without departing from the spirit of the invention.

Claims (10)

1. The acaricidal composition is characterized in that an active ingredient of the acaricidal composition comprises an active ingredient A and an active ingredient B, wherein the active ingredient A is sulfoflumin, the active ingredient B is fluazinam or pyriminostrobin, and the mass ratio of the active ingredient to the active ingredient B is 1:30-42:1.
2. The acaricidal composition according to claim 1, wherein the active ingredient B in the acaricidal composition is fluazinam, the mass ratio of the active ingredient a to the active ingredient B is 1:30-42:1, preferably, the mass ratio of the active ingredient a to the active ingredient B is 1:24-35:1.
3. The acaricidal composition according to claim 1, wherein the active ingredient B in the acaricidal composition is pyriminostrobin, the mass ratio of the active ingredient a to the active ingredient B is 1:28-25:1, preferably, the mass ratio of the active ingredient a to the active ingredient B is 1:15-12:1.
4. The acaricidal composition according to claim 1, wherein the acaricidal composition comprises an agrochemically acceptable auxiliary ingredient in addition to the active ingredient, wherein the auxiliary ingredient is a filler and/or a surfactant.
5. The acaricidal composition according to claim 1, wherein the acaricidal composition is in the form of a solution, a suspension, an emulsifiable concentrate, an aqueous emulsion, a microcapsule suspension, a microemulsion, a suspoemulsion, a dispersible oil suspension, a granule, a water dispersible granule or a wettable powder.
6. The acaricidal composition according to claim 5, wherein the formulation is a suspension, emulsifiable concentrate, water dispersible granule or wettable powder.
7. Use of a acaricidal composition according to any one of claims 1 to 6 for controlling phytophagous harmful mites.
8. The use according to claim 7, wherein the phytophagous pest mites are spider mites.
9. The use according to claim 8, wherein the tetranychus is panonychus citri, panonychus ulmi, tetranychus cinnabarinus or tetranychus urticae.
10. The use according to claim 7, wherein the acaricidal composition is applied to mites and to plants in which they grow or to the environment in which they grow.
CN202311764473.4A 2023-12-21 2023-12-21 Mite-killing composition and application thereof Pending CN117770267A (en)

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